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Hyo‐Sang Do

Observed names: Hyo-Sang Do, Hyosang Do
ORCID: 0000-0002-6903-6357
Observed ORCID: 0000-0002-6903-6357
OpenAlex ID: A5045700299
Enhanced thrombospondin-1 causes dysfunction of vascular endothelial cells derived from Fabry disease-induced pluripotent stem cells
2020 · Hyo-Sang Do, Sang-Wook Park, et al. · EBioMedicine · 43
Therapeutic gene correction for Lesch-Nyhan syndrome using CRISPR-mediated base and prime editing
2023 · Gayoung Jang, Ha Rim Shin, et al. · Molecular Therapy — Nucleic Acids · 19
KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature
2022 · Yunha Choi, Jungmin Choi, et al. · Molecular Genetics & Genomic Medicine · 18
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Dysregulated ECM remodeling proteins lead to aberrant osteogenesis of Costello syndrome iPSCs
2021 · Jong Bin Choi, Joonsun Lee, et al. · Stem Cell Reports · 13
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Fasudil alleviates the vascular endothelial dysfunction and several phenotypes of Fabry disease
2023 · Jong Bin Choi, Dong-Won Seol, et al. · Molecular Therapy · 11
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Genetic heterogeneity of cardiomyopathy and its correlation with patient care
2023 · Mi Jin Kim, Seulgi Cha, et al. · BMC Medical Genomics · 10
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Generation of PDGFRα+ Cardioblasts from Pluripotent Stem Cells
2017 · Seon Pyo Hong, Sukhyun Song, et al. · Scientific Reports · 10
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Identification of a novel therapeutic target underlying atypical manifestation of Gaucher disease
2022 · Eun Na Kim, Hyo‐Sang Do, et al. · Clinical and Translational Medicine · 9
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Variable allelic expression of imprinted genes in human pluripotent stem cells during differentiation into specialized cell types in vitro
2014 · Sang-Wook Park, Jihoon Kim, et al. · Biochemical and Biophysical Research Communications · 9
Clinical and genetic analyses of patients with lateralized overgrowth
2022 · Yoon-Myung Kim, Yena Lee, et al. · BMC Medical Genomics · 8
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Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis: Case reports and a review of the literature
2024 · Jun Hee Cho, Soojin Hwang, et al. · Molecular Genetics & Genomic Medicine · 7
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A 10‐year follow‐up of high‐dose ambroxol treatment combined with enzyme replacement therapy for neuropathic Gaucher disease
2024 · Soojin Hwang, Hyunwoo Bae, et al. · American Journal of Hematology · 6
Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea
2021 · Yena Lee, Yunha Choi, et al. · BMC Medical Genomics · 6
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Beyond CHD7 gene: unveiling genetic diversity in clinically suspected CHARGE syndrome
2025 · Dohyung Kim, Ji-Hee Yoon, et al. · Journal of Human Genetics · 5
Generation of a CRISPR/Cas9-corrected-hiPSC line (DDLABi001-A) from Fabry disease (FD)-derived iPSCs having α-galactosidase (GLA) gene mutation (c.803_806del)
2022 · Jong Bin Choi, Donghyuk Seo, et al. · Stem Cell Research · 4
Case Report: Mevalonic Aciduria Complicated by Acute Myeloid Leukemia After Hematopoietic Stem Cell Transplantation
2021 · Hyery Kim, Beom Hee Lee, et al. · Frontiers in Immunology · 4
Clinical and molecular characteristics of Korean patients with Kabuki syndrome
2024 · Ji-Hee Yoon, Soojin Hwang, et al. · Journal of Human Genetics · 3
Factors Affecting the Genetic Diagnostic Rate in Congenital Heart Disease
2022 · Jun Sung Park, Go Hun Seo, et al. · Congenital Heart Disease · 3
Transcriptional Profiles of Imprinted Genes in Human Embryonic Stem Cells During In vitro Differentiation
2014 · Sang-Wook Park, Hyo-Sang Do, et al. · International Journal of Stem Cells · 3
Expanding genetic and clinical spectra of β-tubulinopathies: A Korean study
2025 · Soojin Hwang, Hyunwoo Bae, et al. · Journal of Human Genetics · 2
Therapeutic effects of lomerizine on vasculopathy in Fabry disease
2025 · Jong Bin Choi, Hyo-Sang Do, et al. · Scientific Reports · 1
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High Prevalence of Genetic Alterations in Infantile-Onset Cardiomyopathy
2021 · Junsung Park, Go Hun Seo, et al. · Congenital Heart Disease · 1
Long-Term Maintenance Therapy with Carglumic Acid in Children with Propionic or Methylmalonic Acidemia: Metabolic and Neurodevelopmental Outcomes
2026 · Soojin Hwang, Beom Hee Lee, et al. · SSRN Electronic Journal
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Ataluren‐Induced Functional Restoration of Neurofibromin in Fibroblasts From Neurofibromatosis Type 1 Patients With Nonsense Mutations
2025 · Soyoung Kim, Hyosang Do, et al. · MedComm
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Clinical and genetic analyses and treatment outcomes of patients with lateralized overgrowth
2022 · Yoon-Myung Kim, Yena Lee, et al. · Research Square
Works count: 28
Citation count: 195
H-index: 9
I10-index: 7
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